Canonical Allele Identifier: CA885812207
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1366239985
MyVariant Identifiers: chr1:g.115256891C>G (hg19) chr1:g.114714270C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714270C>G , CM000663.2:g.114714270C>G GRCh38
NC_000001.10:g.115256891C>G , CM000663.1:g.115256891C>G GRCh37
NC_000001.9:g.115058414C>G NCBI36
NG_007572.1:g.7625G>C , LRG_92:g.7625G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-292G>C MANE Select ENSP00000358548.4:n.112-292G>C
ENST00000369535.4:c.112-292G>C ENSP00000358548.4:n.112-292G>C
NM_002524.4:c.112-292G>C NP_002515.1:n.112-292G>C
NM_002524.5:c.112-292G>C MANE Select NP_002515.1:n.112-292G>C
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